Notch信号通路
免疫印迹
肿瘤坏死因子α
信号转导
川地163
化学
分子生物学
白细胞介素
巨噬细胞极化
流式细胞术
细胞生物学
生物
巨噬细胞
生物化学
细胞因子
体外
免疫学
基因
作者
Xuerui Hu,Bangzhen Hong,Xiaoxiao Shan,Yue Cheng,Daiyin Peng,Rongfeng Hu,Lei Wang,Weidong Chen
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2023-02-24
卷期号:28 (5): 2140-2140
被引量:13
标识
DOI:10.3390/molecules28052140
摘要
The homogeneous galactoglucan PCP-1C extracted from Poria cocos sclerotium has multiple biological activities. The present study demonstrated the effect of PCP-1C on the polarization of RAW 264.7 macrophages and the underlying molecular mechanism. Scanning electron microscopy showed that PCP-1C is a detrital-shaped polysaccharide with fish-scale patterns on the surface, with a high sugar content. The ELISA assay, qRT-PCR assay, and flow cytometry assay showed that the presence of PCP-1C could induce higher expression of M1 markers, including tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and interleukin-12 (IL-12), when compared with the control and the LPS group, and it caused a decrease in the level of interleukin-10 (IL-10), which is the marker for M2 macrophages. At the same time, PCP-1C induces an increase in the CD86 (an M1 marker)/CD206 (an M2 marker) ratio. The results of the Western blot assay showed that PCP-1C induced activation of the Notch signaling pathway in macrophages. Notch1, ligand Jagged1, and Hes1 were all up-regulated with the incubation of PCP-1C. These results indicate that the homogeneous Poria cocos polysaccharide PCP-1C improves M1 macrophage polarization through the Notch signaling pathway.
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